Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
  • C08G75/02—Polythioethers
  • C08G75/0204—Polyarylenethioethers
  • C08G75/025—Preparatory processes

Definitions

• the invention relates to a process for the preparation of high-molecular, optionally branched polyarylene sulphides. These can be prepared without a catalyst in a polar organic solvent by reacting dihalogenoaromatic compounds with mixtures of sodium and potassium sulphides and hydrogensulphides.
• auxiliaries in order to obtain high-molecular polyaryl sulphides.
• auxiliaries can be co-solvents, such as dialkylcarboxamides, or catalysts, such as alkali metal carboxylates, salts of polycarboxylic acids, sulphonic acids, halides, phosphates or phosphonates.
• the invention relates to a process for the preparation, without a catalyst or auxiliaries, of optionally branched polyarylene sulphides from
• Ar is an aromatic or heterocyclic radical
• X represents halogen, such as chlorine or bromine
• n the number 3 or 4
• a polar organic solvent characterized in that the mixture of sodium and potassium sulphides and hydrogen-sulphides contains sodium and potassium ions in a ratio from 95 to 5 up to 5 to 95 mol %, preferably 95 to 5 up to 50 to 50 mol %.
• the reaction time can be varied within a wide range. It can be from less than 1 hour up to several days, preferably from 1 hour up to 48 hours and particularly preferentially 2 to 18 hours.
• the reaction can be carried out continuously or discontinuously.
• the reactants can be initially placed together and reacted.
• Substances containing water can be freed from water separately before the reaction.
• substances containing water it is also possible for substances containing water to be freed from water by distillation in the reaction mixture before the reaction leading to the polymer. It is also possible to meter in the starting substances in portions or to add them successively to the reaction mixture in any desired sequence.
• Meta-dihalogenoaromatic and para-dihalogenoaromatic compounds of the formula (I) or (II) can be employed in accordance with the invention.
• the ratio of meta-dihalogenoaromatic compound to para-dihalogenoaromatic compound can be up to 30:70.
• thermoplastic means It is particularly preferable to employ p-dihalogenoaromatic compounds in order to obtain polyarylene sulphides which can be processed by thermoplastic means.
• Sodium sulphide and potassium sulphide can be prepared from hydrogen sulphide and sodium hydroxide or potassium hydroxide.
• Sodium ions and potassium ions are present in the reaction solution, in accordance with the invention, in a ratio from 95 to 5 up to 5 to 95 mol %, preferably 95 to 5 up to 50 to 50 mol %, relative to the total amount of sodium and potassium ions.
• the molar ratio of sodium to potassium ions according to the invention can be obtained by using either sodium or potassium sulphides or hydrogensulphides. It is also possible, for example, to react sodium hydrogensulphide with potassium hydroxide in an appropriate amount, and vice versa.
• dihalogenoaromatic compounds of the formula (I) to be employed in accordance with the invention are preferably: 1,4-dichlorobenzene, 1,4-dibromobenzene, 1-bromo-4-chlorobenzene, 1,3-dichlorobenzene, 1,3-dibromobenzene and 1-bromo-3-chlorobenzene. They can be used on their own or as a mixture with one another. 1,4-Dichlorobenzene and/or 1,4-dibromobenzene are particularly preferred.
• R 1 in formula II preferably represents hydrogen, C 1 -C 4 -alkyl, C 5 -C 10 -cycloalkyl, C 6 -C 10 -aryl, C 7 -C 14 -alkylaryl or C 7 -C 14 -aralkyl. It is also possible for two radicals R 1 in the ortho-position relative to one another to form a fused aromatic ring having a total of 6 C atoms or a fused heterocyclic ring having 5-6 ring atoms and 1-3 hetero-atoms, such as N, O or S.
• dihalogenoaromatic compounds of the formula (II) to be employed in accordance with the invention: 2,5-dichlorotoluene, 2,5-dichloroxylene, 1,4-dichloro-2-ethylbenzene, 1,4-dibromo-2-ethylbenzene, 1-bromo-4-chloro-2-ethylbenzene, 1,4-dichloro-2,3,5,6-tetramethylbenzene, 1,4-dichloro-2-cyclohexylbenzene, 2,5-dichlorobiphenyl, 2-benzyl-1,4-dichlorobenzene, 2,5-dibromobiphenyl, 2,5-dichloro-4'-methylbiphenyl, 2,5-dibromo-4'-methylbiphenyl, 1,4-dichloro-2-hexylbenzene, 2,4-dichlorotoluene, 2,4-dichlorotol
• Ar preferably represents an aromatic radical having 6-24 C atoms or a heterocyclic radical having 6-24 ring atoms, and particularly preferentially an aromatic radical having 6-10 C atoms or a heterocyclic radical, or can contain up to 3 hetero-atoms, such as N, S and O.
• trihalogenoaromatic and tetrahalogenoaromatic compounds of the formula (III) to be employed in accordance with the invention 1,2,3-trichlorobenzene, 1,2,4-trichlorobenzene, 1,2,4-tribromobenzene, 1,3,5-trichloro-2,4,6-trimethylbenzene, 1,2,3-trichloronaphthalene, 1,2,6-trichloronaphthalene, 2,3,4-trichlorotoluene, 2,3,6-trichlorotoluene, 1,2,3,4-tetrachloronaphthalene, 1,2,4,5-tetrachlorobenzene, 2,2'-4,4'-tetrachlorobiphenyl and 1,3,5-trichlorotriazine.
• lactams such as N-alkyl lactams, for example N-methylpyrrolidone, N-ethylpyrrolidone, N-methylpiperidone, N-isopropylpyrrolidone, N-methylcarprolactam or N-ethylcaprolactam
• cyclic ureas such as 1,3-dimethylimidazolidin-2-one, or other polar organic solvents such as
• the boiling point of the solvents should be 200° C. to 280° C.
• polyarylene sulphides prepared in accordance with the invention can be mixed with other polymers, pigments and fillers, for example graphite, metal powders, glass powders, ground quartz, glass fibres and carbon fibres, or the stabilizers or mould release agents which are customary for polyarylene sulphides can be added to them.
• melt flow behaviour of polyarylene sulphides is measured as specified in ASTM 1239-70 at 316° C. using a 5 kg weight, and is quoted in g/10 minutes.
• melt viscosity can be determined within a very wide range from 10 -1 to 10 7 Pa.s.
• Instron rheometer the polymer is melted between a fixed plate and a rotatable cone and the torque of the cone is determined.
• the melt viscosity as a function of the shear stress, can be calculated from the torque, the angular velocity and the characteristics of the apparatus.
• the model 3250 rheometer made by Instron was used; diameter of the cone and of the plate 2 cm.
• the polyarylene sulphides according to the invention Immediately after being isolated from the reaction mixture, the polyarylene sulphides according to the invention generally have melt viscosities from 0.1 ⁇ 10 1 to 5 ⁇ 10 4 Pa.s, preferably from 0.1 ⁇ 10 2 to 2.5 ⁇ 10 4 Pa.s, and good properties in respect of colour.
• the polyarylene sulphides can also be analysed by chromatographic methods in order to provide information on molecular weight and molecular weight distribution.
• HPLC high pressure liquid chromatography
• GPC gel permeation chromatography
• Customary support materials can be used as the stationary phase, for example Li-Chropren®, Lobar®, Lichorsorb®, Lichrosphor®, Perisorb®, Hibar®, Fractogel®, Fractosil®, Ultrastyragel®, Microstyragel®, Zorbax®, Bondagel® and Shodex®.
• Customary solvents can be used as solvents and mobile phaSes. These Should have an adequate solubility for the polymer.
• Absolute or relative standardizations can be carried out in the chromatographic methods of analysis.
• suitable standard substances for relative standardizations are customary polymers, such as, for example, polystyrene, polyethylene, polyethylene terephthalate, polybutylene terephthalate, polyesters, such as purely aromatic polyesters, polycarbonate, polyamides, such as PA6, PA66 and PA11, polysulphones or polyether-sulphones.
• the chromatography required for the analytical determination of the molecular weights or molecular weight distribution can be carried out under various pressures from 1 to 10 bar.
• the chromatographic determination is carried out at a temperature from room temperature up to 250° C.
• the weight average molecular weights M w are 25,000 to 500,000, preferably 25,000 to 300,000 and particularly preferentially 25,000 to 150,000.
• the polyarylene sulphides can be directly processed by extrusion, blow-extrusion, injection moulding or other customary processing techniques to give films, shaped articles or fibres. These can be used in a customary manner, for example as automobile components, mountings, electrical components, for example switches or electronic panels, components which are resistant to chemicals and stable to weathering and equipment such as pump casings and pump impellers, etching bath trays, sealing rings, parts of office machines and telecommunications devices and also household appliances, valves and ballbearing components.
• Example 2 but with 13.76 mol of sodium ions and no potassium ions.
• a polyarylene sulphide having a melt viscosity ⁇ m >1 Pa.s is obtained in a yield of 87.1%, relative to 1,4-dichlorobenzene.
• Example 1 but with 13.76 mol of potassium ions and no sodium ions.
• a polyarylene sulphide having a melt viscosity ⁇ m >1 Pa.s is obtained in a yield of 83.6%, relative to 1,4-dichlorobenzene.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=6278381

Family Applications (1)

Country Status (4)

Families Citing this family (6)

Citations (3)

Family Cites Families (3)

• 1985
  • 1985-08-13 DE DE19853528977 patent/DE3528977A1/de not_active Withdrawn
• 1986
  • 1986-08-01 US US06/891,656 patent/US4762911A/en not_active Expired - Fee Related
  • 1986-08-01 DE DE8686110674T patent/DE3662149D1/de not_active Expired
  • 1986-08-01 EP EP86110674A patent/EP0215258B1/fr not_active Expired
  • 1986-08-08 JP JP61185414A patent/JPS6239631A/ja active Pending

Patent Citations (3)

Also Published As

Similar Documents

Legal Events